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Title
Chondroitin and Dermatan Sulfate Bioinks for 3D Bioprinting and Cartilage Regeneration
Author
Zabala, Alaitz
Author (from another institution)
Lafuente-Merchan, Markel
Galvez Martin, Patricia
Marchal, Juan Antonio
Vázquez-Lasa, Blanca
Gallego, Idoia
Sáenz-del-Burgo, Laura
Pedraz, José Luis
Research Group
Tecnologías de superficies
Other institutions
Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU)
Bioibérica (Spain)
Universidad de Granada
Biomaterials and Nanomedicine (CIBER-BBN)
Instituto de Investigación Sanitaria Bioaraba
Instituto de Ciencia y Tecnología de Polímeros (ICTP-CSIC)
Version
Postprint
Rights
© 2022 Wiley
Access
Embargoed access
URI
https://hdl.handle.net/20.500.11984/5471
Publisher’s version
https://doi.org/10.1002/mabi.202100435
Published at
Macromolecular Bioscience  Early View. N. artículo 2100435, 2022
Publisher
Wiley
Abstract
Cartilage is a connective tissue which a limited capacity for healing and repairing. In this context, osteoarthritis (OA) disease may be developed with high prevalence in which the use of scaffolds ma ... [+]
Cartilage is a connective tissue which a limited capacity for healing and repairing. In this context, osteoarthritis (OA) disease may be developed with high prevalence in which the use of scaffolds may be a promising treatment. In addition, three-dimensional (3D) bioprinting has become an emerging additive manufacturing technology because of its rapid prototyping capacity and the possibility of creating complex structures. This study is focused on the development of nanocellulose-alginate (NC-Alg) based bioinks for 3D bioprinting for cartilage regeneration to which it is added chondroitin sulfate (CS) and dermatan sulfate (DS). First, rheological properties are evaluated. Then, sterilization effect, biocompatibility, and printability on developed NC-Alg-CS and NC-Alg-DS inks are evaluated. Subsequently, printed scaffolds are characterized. Finally, NC-Alg-CS and NC-Alg-DS inks are loaded with murine D1-MSCs-EPO and cell viability and functionality, as well as the chondrogenic differentiation ability are assessed. Results show that the addition of both CS and DS to the NC-Alg ink improves its characteristics in terms of rheology and cell viability and functionality. Moreover, differentiation to cartilage is promoted on NC-Alg-CS and NC-Alg-DS scaffolds. Therefore, the utilization of MSCs containing NC-Alg-CS and NC-Alg-DS scaffolds may become a feasible tissue engineering approach for cartilage regeneration. [-]
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